| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44674421-44674759 | Common:3; Rare:87 | ||||
| chr1:44775258-44775603 | Common:1; Rare:110 | ||||
| chr1:44775683-44776141 | Common:3; Rare:157 | ||||
| chr1:44777534-44777973 | Common:2; Rare:114 | ||||
| chr1:44800168-44800384 | Common:1; Rare:49 | ||||
| chr1:44986538-44986791 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr1:45339968-45340250 | Rare:101; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr1:45340345-45340418 | Common:1; Rare:18; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:45500046-45500350 | Common:1; Rare:75; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521798-45522077 | Common:1; Rare:106 | ||||
| chr1:45550738-45551123 | Common:3; Rare:92 | ||||
| chr1:45583927-45584200 | Common:1; Rare:105 | ||||
| chr1:45686499-45686577 | Rare:25 | ||||
| chr1:45687017-45687351 | Common:2; Rare:87 | ||||
| chr1:45688038-45688273 | Common:1; Rare:62 |